HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355405Generated: October 29, 2026
Hexamethylenetetramine → 3,5-Difluoro-2,4-dihydroxybenzaldehyde
https://huagongshe.com/reaction/355405
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2,4-Difluororesorcinol | HCID 10844515 | — |
| Product | 3,5-Difluoro-2,4-dihydroxybenzaldehyde | HCID 18942327 | 59% |
Reaction Steps
A solution of 2,4-difluororesorcinol (0.50 g, 3.4 mmol) and hexamethylenetetraamine (0.96 g, 6.8 mmol) in 4 mL trifluoroacetic acid is heated to reflux for 24 hours. After cooling, the reaction is quenched by the addition of 2 mL 20% H2SO4, and then stirred for an additional hour. The reaction mixture is then poured into 50 mL water and extracted with EtOAc (50 mL×2), washed with brine (30 mL), dried over anhydrous MgSO4, and concentrated in vacuo. The residue is purified by sublimation to yield 0.35 g (59%) of Compound 13 as a colorless powder. Mp. 141°-143° C. 1H-NMR (DMSO-d6) δ 9.7 (s, 1H), 7.21 (dd, J=9.8; 6.5 Hz, 1H). 19 F-NMR(DMSO-d6) Φ 143.78 (t, J=9.8 Hz, 1F), 158.31 (d, J=6.5 Hz, 1F). Anal. calcd for C7H4F3O3 : C, 48.29; H, 2.32. Found: C, 47.87, H, 2.62.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05830912 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-68f75e9935eb40d284fac4d0c4413604 |
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| Source note | uspto-grants-1998_11 |
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